A clinical trial to assess the pharmacokinetics, safety, and food effect of AD-230 in healthy adults
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
24
AD-230 1Tab., Per Oral, Fasted
AD-230 1 Tab., Per Oral, Fed state
Kyungpook National university hospital
Daegu, South Korea
Area under the plasma concentration-time curve during dosing interval (AUCt)
Time frame: -24hours to 72hours
Maximum concentration of drug in plasma (Cmax)
Time frame: -24hours to 72hours
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